1917306-14-9

1917306-14-9 structure
1917306-14-9 structure
  • Name: JNJ-61803534
  • Chemical Name: JNJ-61803534
  • CAS Number: 1917306-14-9
  • Molecular Formula: C23H23Cl2F6N3O4S
  • Molecular Weight: 622.41
  • Catalog: Signaling Pathways Metabolic Enzyme/Protease ROR
  • Create Date: 2023-04-05 14:53:25
  • Modify Date: 2024-07-08 18:55:46
  • JNJ-61803534 is a potent and orally active RORγt inverse agonist with an IC50 of 9.6  nM. JNJ-61803534 has anti-inflammatory activity. JNJ-61803534 inhibits IL-17A production in human CD4+ T cells under Th17 differentiation conditions[1].

Name JNJ-61803534
Description JNJ-61803534 is a potent and orally active RORγt inverse agonist with an IC50 of 9.6  nM. JNJ-61803534 has anti-inflammatory activity. JNJ-61803534 inhibits IL-17A production in human CD4+ T cells under Th17 differentiation conditions[1].
Related Catalog
Target

RORγt

In Vitro JNJ-61803534 在转染了编码 RORγt 载体的 HEK-293 T 细胞中抑制 RORγt 转录,IC50 为 9.6 nM[1]。 JNJ-61803534 (1 nM-1 μM) 抑制人血液中分离的 CD4+ T 细胞产生 IL-17A、IL-17F IFNγ 和 IL-22[1]。 JNJ-61803534 不影响 CD4+ T 细胞的体外 Treg 分化[1]。
In Vivo JNJ-61803534 (100 mg/kg,口服) 抑制小鼠血液中体外刺激产生的 IL-17A[1]。 JNJ-61803534 (3-100 mg/kg BID 或 60 mg/kg QD,p.o.) 减轻小鼠胶原诱导性关节炎 (CIA) 模型的炎症、软骨损伤和骨质破坏[1]。 JNJ-61803534 (30 和 100 mg/kg,口服) 减轻小鼠 Imiquimod (HY-B0180) 诱导的皮肤银屑病样炎症[1]。 Animal Model: Mouse collagen-induced arthritis (CIA) model[1] Dosage: 3-100 mg/kg BID or 60 mg/kg QD Administration: Oral administration (p.o.) Result: Decreased clinical arthritis scores and hind paw histopathology scores.
References

[1]. Xue X, et al. Preclinical and clinical characterization of the RORγt inhibitor JNJ-61803534. Sci Rep. 2021 May 26;11(1):11066.  

Molecular Formula C23H23Cl2F6N3O4S
Molecular Weight 622.41
Storage condition 2-8°C